First report of inherited thyroxine-binding globulin deficiency in Iran caused by a known de novo mutation in SERPINA7

MLA

Fahimeh Soheilipour, et al. “First Report of Inherited Thyroxine-Binding Globulin Deficiency in Iran Caused by a Known de Novo Mutation in SERPINA7.” Molecular Genetics and Metabolism Reports, vol. 8, no. C, Sept. 2016, pp. 13–16. EBSCOhost, https://doi.org/10.1016/j.ymgmr.2016.06.001.

APA

Fahimeh Soheilipour, Hassan Fazilaty, Fatemeh Jesmi, William A. Gahl, & Babak Behnam. (2016). First report of inherited thyroxine-binding globulin deficiency in Iran caused by a known de novo mutation in SERPINA7. Molecular Genetics and Metabolism Reports, 8(C), 13–16. https://doi.org/10.1016/j.ymgmr.2016.06.001

Chicago

Fahimeh Soheilipour, Hassan Fazilaty, Fatemeh Jesmi, William A. Gahl, and Babak Behnam. 2016. “First Report of Inherited Thyroxine-Binding Globulin Deficiency in Iran Caused by a Known de Novo Mutation in SERPINA7.” Molecular Genetics and Metabolism Reports 8 (C): 13–16. doi:10.1016/j.ymgmr.2016.06.001.